Mondo Disease Ontology
1299 terms(s) returned
Term Type: Class | Record: 1001 to 1050 of 1299 Records | Page: 21 of 26, First Previous Next Last | Show Records Per Page |
- gluten
- gluten refined food product
- gluthathione peroxidase deficiency
- glycan
- glycemic agent therapy
- glyceraldehyde-3-phosphate dehydrogenase (NAD(P)+) (phosphorylating) activity
- glyceraldehyde-3-phosphate dehydrogenase deficiency
- glycerol ether biosynthetic process
- glycerol ether metabolic process
- glycerol kinase activity
- glycerol kinase deficiency, adult form
- glycerol kinase deficiency, infantile form
- glycerol kinase deficiency, juvenile form
- glycerol metabolic process
- glycerol metabolism disease
- glycerolipid biosynthetic process
- glycerolipid metabolic process
- glyceronephosphate O-acyltransferase deficiency
- glycerophospholipid biosynthetic process
- glycerophospholipid metabolic process
- glycine N-methyltransferase deficiency
- glycine amidinotransferase activity
- glycine encephalopathy
- glycine encephalopathy 1
- glycine encephalopathy 2
- glycine metabolic process
- glycine metabolism disease
- glycogen biosynthetic process
- glycogen catabolic process
- glycogen metabolic process
- glycogen storage disease I
- glycogen storage disease II
- glycogen storage disease III
- glycogen storage disease IXa1
- glycogen storage disease IXa2
- glycogen storage disease IXb
- glycogen storage disease IXc
- glycogen storage disease IXd
- glycogen storage disease Ib
- glycogen storage disease Id
- glycogen storage disease V
- glycogen storage disease VI
- glycogen storage disease VII
- glycogen storage disease XV
- glycogen storage disease due to GLUT2 deficiency
- glycogen storage disease due to acid maltase deficiency, infantile onset
- glycogen storage disease due to acid maltase deficiency, late-onset
- glycogen storage disease due to aldolase A deficiency
- glycogen storage disease due to glucose-6-phosphatase deficiency type IA
- glycogen storage disease due to glycogen branching enzyme deficiency